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  2. Ethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_sulfate

    ch 3 ch 2 oh + h 2 so 4 → ch 3 ch 2 oso 3 h + h 2 o If the temperature exceeds 140 °C, the ethyl sulfate product tends to react with residual ethanol starting material, producing diethyl ether . If the temperature exceeds 170 °C in a considerable excess of sulfuric acid, the ethyl sulfate breaks down into ethylene and sulfuric acid.

  3. Diethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_sulfate

    In preparing ethyl esters of fatty acids, both equivalents of the ethyl electrophile are transferred, unlike the usual alkylation of phenoxides: [1] 2 RCO 2 Na + (C 2 H 5 O) 2 SO 2 → 2 RCO 2 C 2 H 5 + Na 2 SO 4. Both dimethyl sulfate and diethyl sulfate react with inorganic nucleophiles as well. For example, potassium iodide gives ethyl iodide.

  4. Ferric subsulfate solution - Wikipedia

    en.wikipedia.org/wiki/Ferric_subsulfate_solution

    Ferric subsulfate (also known as Monsel's solution) is often used by Jewish burial societies (chevra kadisha) to stop post-mortem bleeding.Since Jewish burial does not allow any external skin adhesives such as bandages, tape, glue or resin, ferric subsulfate is an effective way to stop post-mortem bleeding.

  5. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    Sulfate is an inert anion, so nature activates it by the formation of ester derivative of adenosine 5'-phosphosulfate (APS) and 3'-phosphoadenosine-5'-phosphosulfate (PAPS). Many organisms utilize these reactions for metabolic purposes or for the biosynthesis of sulfur compounds required for life. [ 9 ]

  6. Ethanethiol - Wikipedia

    en.wikipedia.org/wiki/Ethanethiol

    Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...

  7. Polystyrene sulfonate - Wikipedia

    en.wikipedia.org/wiki/Polystyrene_sulfonate

    Polystyrene sulfonic acid, the acid whose salts are the polystyrene sulfonates, has the idealized formula (CH 2 CHC 6 H 4 SO 3 H) n. The material is prepared by sulfonation of polystyrene: (CH 2 CHC 6 H 5) n + n SO 3 → (CH 2 CHC 6 H 4 SO 3 H) n. Several methods exist for this conversion, which can lead to varying degree of sulfonation.

  8. Color Developing Agent 3 - Wikipedia

    en.wikipedia.org/wiki/Color_Developing_Agent_3

    The third in the series of color developing agents used in developing color films, commonly known as CD-3, is chemically known as N-[2-[(4-Amino-3-methylphenyl)ethylamino]ethyl]methanesulfonamide Sesquisulfate Monohydrate. [1]

  9. Sodium 2-hydroxyethyl sulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_2-hydroxyethyl...

    Sodium 2-hydroxyethyl sulfonate (also: sodium isethionate) is the sodium salt of 2-hydroxyethane sulfonic acid (isethionic acid), it is used as a hydrophilic head group in washing-active surfactants, known as isethionates (acyloxyethanesulfonates) due to its strong polarity and resistance to multivalent ions.